Using magnetic resonance imaging and diffusion tensor imaging to assess brain damage in alcoholics.

Brain imaging using conventional magnetic resonance imaging (MRI) has revealed that several brain structures in people with a history of chronic alcohol dependence are smaller in volume than the same brain structures in nonalcoholic control subjects. Areas that are particularly affected are the frontal lobes, which are involved in reasoning, judgment, and problem solving. Older people are especially vulnerable to the damaging effects of alcohol. It is unclear whether women show consistently more vulnerability to these changes in the brain than men do. In general, alcoholics evaluated before and after a period of abstinence show some recovery of tissue volume, whereas alcoholics evaluated again after continued drinking show further reductions in brain tissue volume. A new MR technique called diffusion tensor imaging (DTI) can aid in detecting the degradation of fibers (i.e., white matter) that carry information between brain cells (i.e., gray matter). With DTI, researchers studying alcoholics have been able to detect abnormalities in white matter not visible with conventional MRI. Ultimately DTI may be useful in elucidating the mechanisms that underlie macrostructural and functional brain changes seen with abstinence and relapse.


tracts).
can be used to detect and quantify grayand white-matter abnormalities on composition (gray vs. white matter) the integrity of white-matter tracts that body is composed primarily of fat and of the fact that water molecules in the ence (i.e., extent to which fibers align Areas where multiple white-matter tracts cross in different orientations, such as adjacent to the genu of the corpus callosum on axial view, appear lower in intensity because no single orientation predominates.

Coronal Sagittal
Internal Capsule Fornix Axial: sliced along the horizontal plane Coronal: sliced vertically, looking at the brain from the front or back Sagittal: sliced vertically, looking at the brain from the side Genu i

Splenium i
Internal capsule cortex is connected with the brain stem and spinal cord Corpus callosum: a band of white-matter fibers linking the brain's hemispheres Fornix: a pathway that carries information in the brain between the hippocampus and the mamillary bodies Pons: a largely white-matter structure of the brain stem Coronal Axial Sagittal different brain regions (i.e., white-matter Imaging in living patients (i.e., in vivo) both macrostructural and microstructural levels. Conventional structural magnetic resonance imaging (MRI) reveals the size, shape, and tissue of the brain and its constituent parts. Diffusion tensor imaging (DTI) reveals link regions of the brain to each other.
MRI is based on the observation that the protons of hydrogen atoms, when placed in a strong magnetic field, can be detected by manipulating the magnetic field. Because the human water, it is made up mostly of hydrogen atoms. Variations in behavior of hydrogen atoms in different brain tissue types and structures show up as intensity differences that clinical structural MRI can detect and map to visualize and measure gross brain neuroanatomy.
Diffusion tensor imaging makes use brain are always moving-that is, they are in Brownian motion. DTI detects the diffusion, or Brownian movement, of water protons within and between individual cells and yields measures of the magnitude and predominant orientation of this movement. The diffusion properties of water molecules within and between the three-dimensional elements, called voxels, that make up an image reveal the orientation and coher-(sagittal) orientations. Regions of higher intensity represent white-matter tracts. Examples of white-matter tracts are labeled.

Viewing the Brain
: front reg on of the corpus callosum : back reg on of the corpus callosum : the major route by which the cerebral together) of fibers making up whitematter tracts.
Both MRI and DTI have been applied to the study of alcoholism. Structural MRI has been used for more than a decade to detect gross structural changes, such as tissue shrinkage and its reversal, and has identified brain regions that are particularly vulnerable to the toxic effects of chronic alcohol consumption. DTI, the more recently developed technique, is beginning to reveal microstructural abnormalities in white matter that are consistent with post mortem observations of whitematter damage, such as myelin loss, enlargement of microtubules (small tubular structures found inside nearly all cells), and degradation of membranes, even when that white-matter region appears normal on structural MRI.

Structural MRI
Structural MRI studies of patients with chronic alcoholism are generally consis tent with the literature on neuropathology and typically reveal reduced volume of both gray matter and white matter in the cerebral cortex, the folded outer layer of the brain. Older alcoholics show greater volume deficits relative to age-matched control subjects than younger alcoholics, suggesting that the older brain is more vulnerable to the effects of alcohol (Pfefferbaum et al. 1992). MRI usually shows that the greatest loss occurs in the frontal lobes, which are used in reasoning, working memory, and problem solving (Pfefferbaum et al. 1997). Changes also appear in other structures involved in memory, such as the hippocampus, mamillary bodies, thalamus, and cerebellar cortex (for a review, see Sullivan 2000).
Alcoholic men (Pfefferbaum et al. 1996) and women (Hommer et al. 1996) also show thinning of the corpus callo sum, a band of white-matter fibers link ing the brain's hemispheres. Reduced volume also is reported in the pons, a largely white-matter structure of the brain stem that forms a critical node in multiple circuits linking the cerebellum-which regulates balance, posture, movement, and muscle coordinationto cortical regions of the brain involved in motor and sensory processing, as well as regions where these inputs are inte grated (Sullivan et al. 2003). Alcoholics, particularly those with a history of seizures, show reduced white-matter volume in the temporal lobes (Sullivan et al. 1996). Alcoholics also have reduced white-matter volume in a part of the cerebellum known as the cerebellar vermis, where the loss is associated with deficits in postural stability (Sullivan et al. 2000). Lastly, chronic alcohol consumption can lead to specific neurological disorders involving white matter, such as Marchiafava-Bignami disease and central pontine myelinolysis (Charness 1993).
Certain structural MR images of alcoholics show areas of greater bright ness in white matter, called white-matter hyperintensities (WMHIs) (Jernigan et al. 1991). These WMHIs can reflect a variety of underlying processes-including swelling caused by excess fluid (i.e., edema), the removal of the myelin sheath (i.e., demyelination), excess cell growth (i.e., gliosis), and increased extracellular fluid-some of which may eventually be documented and eluci dated using DTI.
Long-term MRI studies of alcoholics in recovery or relapse have identified cortical white-matter volume as partic ularly amenable to recovery with absti nence (Shear et al. 1994) or vulnerable to further decline with continued drinking (Pfefferbaum et al. 1995;Pfefferbaum et al. 1998). How volume is restored through abstinence or continues to decline with continued drinking remains unclear but probably involves changes in both myelination and axonal integrity. When motion is unconstrained, as in the large fluid-filled spaces deep in the brain (i.e., the ventricles, as illustrated in the MR image on the left), diffusion is isotropic, which means that motion occurs equally and randomly in all directions. (B) When motion is constrained, as in white-matter tracts (illustrated on the right), diffusion is anisotropic, meaning that motion is oriented more in one direction than another (e.g., along the y axis rather than along the x axis). Most early brain imaging studies of (cerebrospinal fluid [CSF]). Other associated with excessive alcohol use, as alcoholism were confined to male sub-studies have not supported the idea of indicated by both post mortem and in jects. More recently, researchers have increased vulnerability among women vivo studies. sought to determine whether women's (Pfefferbaum et al. 2001). These later Conventional MR images are "pic brains are more or less vulnerable than MRI studies highlight the importance tures" primarily of free water, the concenmen's to the damaging effects of alcohol of controlling adequately for gender tration of which differs by tissue type: abuse or dependence. A neuroimaging related differences in body/brain mor-White matter consists of about 70 perstudy that used computerized tomogra phology and quantity and pattern of cent water, gray matter 80 percent, and phy (CT) showed comparable deficits drinking. Furthermore, it is becoming CSF 99 percent. These differences in in men and women, even though the increasingly apparent that brain tissue, water content contribute to the contrast women drank much less alcohol than especially white matter, that appears norbetween tissue types visible on structural the men (Jacobson 1986). This find-mal on MRI in alcoholic patients may in images. DTI takes this imaging further ing, which suggested that women were fact be affected by alcoholism. by measuring differences in the freedom more vulnerable to alcohol-induced with which water molecules move within brain damage, has been supported by some MRI studies (Hommer et al.

Diffusion Tensor Imaging
a tissue type and the amount and ori entation of their diffusion, especially in 2001) measuring volumes of cortical white matter. With appropriate data white and gray matter and the fluid DTI shows particular promise for collection and processing techniques that bathes the brain and spinal cord assessing white-matter damage that is (Adalsteinsson et al. 2002), researchers  Water molecules are in constant motion. In regions such as the ventri cles, relatively large fluid-filled spaces deep in the brain, which offer few or no physical constraints, movement occurs randomly in every direction. This random movement is described as isotropic (iso meaning "same" and tropic meaning "movement"). By con trast, water molecules in white-matter fibers are constrained by the physical boundaries of the axon sheath, which cause greater movement along the long axis of the fiber than across it. This movement is called anisotropic (aniso meaning "not the same") (see figure 1).

Alcoholic Man
How do we detect water diffusion in the brain with imaging? One way is to apply extra magnetic field gradients (i.e., diffusion gradients) during image acquisition to yield what is called a diffusion-weighted image. This process is analogous to looking through a microscope, focusing on some relatively motionless solid structures and some particles that are in Brownian motion, unfocusing briefly, and then refocusing the microscope on the same location. The solid structures will come back into focus, but some of the freely moving particles that have moved will be out of focus. In the ventricles, molecules are free to move out of focus. In the whitematter tracts, where axon sheaths restrict movement to one primary direction, it is less likely that molecules will move out of focus (i.e., there is less diffusion). Unlike the microscope, which has only one focus/unfocus direction, the scan ner can focus and refocus in multiple dimensions by applying diffusion gra dients in different directions. The researcher collects one image without gradients and then six images, each with diffusion gradients applied in a different direction (see figure 2).
The technique is called diffusion tensor imaging because a tensor, a mathematical description of the orien tation and magnitude of diffusion, is computed for each voxel from the seven images. Further calculations result in three summary measures that reflect the magnitude or amount of diffusion in each direction. Trace images are based on the average diffusion in all three direc tions and illustrate the overall magnitude of diffusion; in trace images, the ventricles, which contain few obstructions to move ment, are bright, and the gray matter and white matter are both dark (see figure 3).
Fractional anisotropy (FA) images are based on the extent to which one direction dominates; they illustrate the degree to which water molecules move in one predominant orientation. If dif fusion is unconstrained (i.e., isotropic), FA is close to zero. If diffusion has one primary orientation (i.e., is anisotropic), FA can approach 1. Because diffusion follows their orientation, the long, thin, cable-like bundles of fibers making up white-matter tracts appear bright on the FA image (see figure 3).
FA images acquired in different planes will highlight different whitematter tracts or provide different views of them (see the textbox, "Viewing the Brain"). Within a uniformly oriented tract, anything that disrupts the regular structure of white matter, such as loss of the protective myelin sheath or dete rioration of the axons, might allow the water molecules to move more freely, resulting in decreased FA. Thus, lowerthan-expected FA (which would indicate more isotropic diffusion) in a whitematter region of normal volume may reflect the loss of white-matter integrity resulting from a number of conditions, including aging and alcoholism.
In order to link FA values to specific white-matter structures and regions, the FA image should be aligned with an independently collected high-resolution structural MR image that provides the template for defining the white-matter regions of interest (see figure 4). This is the best approach to confirm that the FA values are in fact located in whitematter regions and requires special techniques to ensure accurate and valid matching of FA and structural images (Pfefferbaum et al. 2000b, Pfefferbaum andSullivan 2003).
Another measure that can be com puted with DTI is intervoxel (i.e., between voxels) rather than intravoxel (i.e., within voxel) coherence. This is the degree to which diffusion in neighbor ing voxels has a common orientation (Pfefferbaum et al. 2000b). This measure is similar to FA but views coherence on a larger spatial, voxel-to-voxel scale (in contrast with FA's intravoxel scale).

Application to Alcoholism
Although DTI has revealed white-matter abnormalities in certain neuropsychiatric conditions such as Alzheimer's disease, schizophrenia, AIDS, and depression, as well as in normal aging (for review, see Sullivan and Pfefferbaum 2003), DTI has only recently been used to examine brain white-matter microstruc tural integrity in alcoholism. Selective white-matter degradation associated with alcoholism is well established from neuropathological reports (e.g., Harper The colored bars represent the means, and the represents the standard errors of fractional anisotropy (FA) in three white-matter brain regions in 15 alcoholic men, 12 alcoholic women, and 49 healthy control men and women. As indicated by the stars, the alcoholic men and women had lower regional FA in the genu of the corpus callosum and the centrum semiovale (the mass of white matter composing the interior of the cerbral hemispheres). Only the alcoholic men had lower FA than control subjects in the splenium, as noted by the cross. Research using DTI shows that, rel ative to age-matched control subjects, alcoholic men have lower regional FA, meaning that diffusion is less oriented in a single direction, in the front part (genu) of the corpus callosum and in the mass of white matter that composes the interior of the cerebral hemisphere (the side of the cerebrum; i.e., the cen trum semiovale) (Pfefferbaum et al. 2000a) (see figure 5).
These DTI-detected white-matter abnormalities were functionally relevant; working memory correlated positively with FA in the white-matter region in the back part of the corpus callosum (i.e., the splenium), whereas attention scores correlated positively with intravoxel coherence in the genu (Pfefferbaum et al. 2000a). A study of alcoholic women revealed regional abnormalities in whitematter microstructure (see figure 5) not detectable with MRI macrostructural measures of size . These results provide in vivo evidence that alcoholism disrupts white-matter microstructure and suggest that the interruption of both intra-and inter voxel coherence contributes to deficits in attention and working memory associated with chronic alcoholism. It remains to be determined whether DTI measures of white-matter integrity parallel the increase in white-matter volume that has been associated with maintain ing abstinence (Shear et al. 1994) or the further decrease of white-matter vol ume associated with relapse after detox ification (Pfefferbaum et al. 1995).

Conclusion
Conventional MRI and DTI modalities each quantify different aspects of brain macrostructure and microstructure. When used together to assess patients when they first stop chronic heavy drinking, and again after longer periods of sobriety or possible relapse, MRI and DTI represent a powerful means of characterizing brain changes at different stages of alcoholism. The different types of information provided can be used to test hypotheses about the factors underlying improvement with prolonged abstinence from alcohol or deterioration with resumption of drinking. For example, low levels of FA in white matter may signify reversible demyelination and axonal deterioration or permanent axonal degeneration. If retesting shows an increase in FA (i.e. increased orientation in one direction), this may suggest remyelina tion or regrowth of neuronal processes.
Behavioral studies could include tests that assess functions of cortical regions connected by the white-matter pathways found to be disrupted by alcoholism and then improved with abstinence. Patterns of recovery and deterioration derived from such in vivo neuroimaging studies may provide clues to cellular mechanisms underlying reversible and permanent brain structural and func tional changes occurring during the course of alcoholism. ■